From Wikipedia, the free encyclopedia
(Redirected from Tetramethoxyamphetamine)
Chemical compound
Pharmaceutical compound
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Clinical data | |
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Other names | TeMA; TA |
Legal status | |
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PubChem CID | |
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UNII | |
ChEMBL | |
CompTox Dashboard (EPA) | |
Chemical and physical data | |
Formula | C13H21NO4 |
Molar mass | 255.314 g·mol−1 |
3D model (JSmol) | |
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(verify) |
Tetramethoxyamphetamine (TeMA), or 2,3,4,5-tetramethoxyamphetamine, is a lesser-known psychedelic drug and a substituted amphetamine. Tetramethoxyamphetamine was first synthesized by Alexander Shulgin. In his book PiHKAL (Phenethylamines i Have Known And Loved), the minimum dosage is listed as 50 mg, and the duration unknown. Tetramethoxyamphetamine produces a threshold, mydriasis, and a headache. Limited data exists about its pharmacological properties, metabolism, and toxicity.[1][2][3]
See also
[edit]- Substituted methoxyphenethylamine
- 2,3,4,5-Tetramethoxyphenethylamine (TeMPEA)
- 2,5-Dimethoxy-3,4-methylenedioxyamphetamine (DMMDA)
References
[edit]- ^ Kier LB, Hall LH (December 1977). "Structure-activity studies on hallucinogenic amphetamines using molecular connectivity". Journal of Medicinal Chemistry. 20 (12): 1631–6. doi:10.1021/jm00222a019. PMID 592329.
- ^ Clare BW (February 1990). "Structure-activity correlations for psychotomimetics. 1. Phenylalkylamines: electronic, volume, and hydrophobicity parameters". Journal of Medicinal Chemistry. 33 (2): 687–702. doi:10.1021/jm00164a036. PMID 2299636.
- ^ Clare BW (September 1998). "The frontier orbital phase angles: novel QSAR descriptors for benzene derivatives, applied to phenylalkylamine hallucinogens". Journal of Medicinal Chemistry. 41 (20): 3845–56. doi:10.1021/jm980144c. PMID 9748359.
External links
[edit]![]() | This psychoactive drug-related article is a stub. You can help Wikipedia by expanding it. |
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